Iris Lee

Cronkhite-Canada syndrome (CSS) Description, Causes, and Treatment Protocol

Cronkhite-Canada syndrome (CSS): Description, Causes, and Treatment Protocol

Cronkhite-Canada syndrome (CSS): Description, Causes, and Treatment Protocol Description In 1955, Wilma J. Canada and Leonard W. Cronkhite Jr. initially identified the rare, non-inherited gastrointestinal condition known as CSS. CSS is distinguished by a particular clinical trio of alopecia, i.e., hair loss, gastrointestinal polyps, and onychodystrophy, i.e., nail abnormalities, which is frequently accompanied by numerous

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IgA nephropathy.

IgA nephropathy / Berger’s disease: Description, Causes, and Treatment Protocol

Description IgA nephropathy, commonly known as Berger’s disease, constitutes one of the most prevalent varieties of glomerulonephritis, a collection of kidney disorders affecting the glomeruli. Glomeruli are the small blood arteries in the kidneys that are in charge of removing waste materials and extra fluid from circulation. The accumulation of immunoglobulin A (IgA) deposition in

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